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Organization name
UDI-DI code
Reference / catalog number

6090 — Class III MDR by Diaco Biofarmaceutici srl

MD Atlas
Diaco Biofarmaceutici srl

EUDAMED last updated this device on Mar 2, 2026

6090

805902020FILLERHCL3G

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Diaco Biofarmaceutici srl
UDI-DI code: 08059020201326
Reference / catalog number: 6090

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View device family (Basic UDI)

Manufacturer information

Organization name: Diaco Biofarmaceutici srl
SRN: IT-MF-000012117
Manufacturer status: Active

Related devices

6097805902020FILLERHC4On the market 6095805902020FILLERHC4On the market 6093805902020FILLERHC4On the market 6053805902020FILLERHC4On the market 6094805902020FILLERHC4On the market

Certificates

Certificate health across this manufacturer's portfolio.

CVD005326Issued
Technical documentationNotified body: 0373Expiry: Feb 11, 2031
CVD005226Issued
Technical documentationNotified body: 0373Expiry: Feb 11, 2031
CSQ0033260126Supplemented
Quality management systemNotified body: 0373Expiry: Feb 11, 2031

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08059020201326
Basic UDI-DI: 805902020FILLERHCL3G
Reference / catalog number: 6090
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: senza aghi
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Content — 90 MU37
3 MU48

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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